PHYSICA KR Left Tibial Liner (REF 6532.50.510)Recalls & reported problems
Limacorporate SPA · KR Liner Left #5 - h. 10 · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 08033390089395), received between Mar 16, 2026 and Mar 16, 2026 — classified as 1 injury.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Implant Pain1
- Loss of Range of Motion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 16, 2026Adverse Event Without Identified Device or Use Problem
REVISION SURGERY WAS PERFORMED ON (B)(6) 2021 DUE TO LOSS OF RANGE OF MOTION AND CONTINUAL PAIN DUE TO SCAR TISSUE. SYMPTOMS WERE REPORTED BY PATIENT DURING ANNUAL FOLLOW-UP. ORIGINAL SURGERY WAS PERFORMED ON (B)(6) 2018 TO IMPLANT FOLLOWING KNEE PROSTHETIC COMPONENTS: PHYSICA FIXED TIBIAL PLATE #5 (PART NUMBER 6522.15.050, LOT 1712528, STERILIZATION (B)(4), PHYSICA KR TIB. LINER LEFT #5 (PART NUMBER 6532.50.510, LOT 15AT0VB, STERILIZATION (B)(4), PHYSICA KR FEMUR COMP. LEFT #6 (PART NUMBER 6511.09.560, LOT 17AS0FY, STERILIZATION (B)(4), PHYSICA PATELLA PROSTH. D.35MM (PART NUMBER 6595.50.035, LOT 17AT0DS, STERILIZATION (B)(4). COMPONENTS WERE ORIGINALLY EXPLANTED ON (B)(6) 2021 AND AROUND ONE MONTH LATER NEW PHYSICA KR COMPONENTS WERE IMPLANTED TO RESTORE KNEE FUNCTIONALITY. SURGERY WAS COMPLETED AS INTENDED. PATIENT IS FEMALE. THE EVENT OCCURRED IN THE UNITED STATES.
Patient problems: Implant Pain; Loss of Range of Motion
MAUDE report 24603379 ↗
Other Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer devices
- R3 71363077Smith & Nephew, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER461 reports
- NA 71364009Smith & Nephew, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER174 reports
- JOURNEY 74012415Smith & Nephew, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER163 reports
- JOURNEY 74012416Smith & Nephew, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER163 reports
- JOURNEY 74012414Smith & Nephew, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER129 reports
- GENESIS II 71440194Smith & Nephew, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER114 reports
- GENESIS II 71440842Smith & Nephew, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER113 reports
- JOURNEY 74018901Smith & Nephew, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER106 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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